Senior Director, Business Development
Cincinnati, Oh, Us
Medpace is a full-service Clinical Research Organization (CRO) known for its therapeutic and regulatory excellence in drug and medical device clinical development. We build strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to approval. • Full-service model: Medpace approaches clinical research with a disciplined process that delivers quality results, maximizes efficiencies and accelerates drug and device development. • Unique physician-managed approach: Medpace physicians are fully engaged throughout the entire study. They provide strategic direction for study design and planning, train operational staff, work with primary investigators, provide medical monitoring, and meet with regulatory agencies. This depth of leadership and engagement ensures your trials start and stay on the right path. • Comprehensive global regulatory leadership: Located in the U.S. and Europe, Medpace regulatory experts have the experience to successfully navigate local, national, regional and international regulations, and accelerate the approval process. • Operational team continuity: Your studies are assigned the best team and, with turnover rates that are lower than the industry standard, that team is with you from project initiation to completion. Our global operational staff proactively identify potential issues and provide solutions, ensuring your sites and studies are managed effectively and efficiently. • Excellent, long-term relationships with sites and key opinion leaders: In the competition for the best sites that achieve the best results, these relationships are key to the success of your trial. • Online study management tool: Sponsors, sites and study teams have real-time, web-based access to all study data through ClinTrak®, Medpace’s proprietary suite of study management tools. Visit Medpace.com for details.